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Hypothalamic asymmetry in hemisphere-specific neuroendocrine signaling

Hiroyuki WatanabeDepartment of Pharmaceutical Biosciences, Uppsala University, Uppsala, SwedenYaromir KobikovResearch Affiliate, Department of Pharmaceutical Biosciences, Uppsala University. Present address: Tashkent, UzbekistanOlga NosovaDepartment of Pharmaceutical Biosciences, Uppsala University, Uppsala, SwedenAlisa LukoyanovaNeuronal Networks Group, i3S-Institute for Research and Innovation in Health, University of Porto, Porto, PortugalDaniil SarkisyanDepartment of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, SwedenEmma LindströmDepartment of Pharmaceutical Biosciences, Uppsala University, Uppsala, SwedenVladimir GalatenkoEvotec International GmbH, Göttingen, GermanyYoichi UetaDepartment of Physiology, School of Medicine, University of Occupational and Environmental Health, JapanTakashi MaruyamaDepartment of Physiology, School of Medicine, University of Occupational and Environmental Health, JapanAlfhild GrӧnbladhDepartment of Pharmaceutical Biosciences, Uppsala University, Uppsala, SwedenMathias HallbergDepartment of Pharmaceutical Biosciences, Uppsala University, Uppsala, SwedenJens SchouenborgNeuronano Research Center, Department of Experimental Medical Science, Lund University, Lund, SwedenRui Francisco FerreiraMaster’s course in Biochemistry, Faculty of Sciences, University of Porto, Porto, PortugalSusana Maria SilvaCINTESIS@RISE, Porto, PortugalNikolay LukoyanovNeuronal Networks Group, i3S-Institute for Research and Innovation in Health, University of Porto, Porto, PortugalIgor LavrovDepartment of Neurology, Mayo Clinic, Rochester, MN, USAMengliang ZhangDepartment of Molecular Medicine, University of Southern Denmark, Odense, DenmarkGeorgy BakalkinDepartment of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden
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ABSTRACT Brain lesions classically cause contralateral sensorimotor and postural deficits, attributed to the decussation of descending neural pathways. However, recent findings reveal that, beyond neural mechanisms, contralateral effects can also be mediated by the neuroendocrine system via humoral pathways. This raises the possibility that the brain regulates left- and right-sided peripheral processes through hypothalamic neurohormones released into the bloodstream. For such spatially targeted endocrine signaling to occur, hemisphere-specific neural activity must be encoded into side-specific hormonal output—requiring a lateralized organization of hypothalamic neuroendocrine systems. Here, we report molecular asymmetries in the rat hypothalamus that support this mechanism. Transcriptomic analysis revealed asymmetric expression of eleven neurohormonal genes, including Gnrh1 , Cck , and Trh , along with distinct left-right side-specific gene co-expression networks. Chemogenetic stimulation of Arg-vasopressin neurons in vasopressin-hM3Dq-mCherry transgenic rats produced generalized changes in these networks—predominantly in the right hypothalamus—suggesting that hypothalamic neurohormonal circuits function as integrated, lateralized ensembles. Stereological analysis revealed asymmetric coordination of vasopressin neurons within the paraventricular nucleus, with the left rostral region decoupled from the right rostral and caudal subregions. Functionally, gonadotropin-releasing hormone, cholecystokinin-8, and thyrotropin-releasing hormone—administered intracisternally in rats with complete spinal cord transection—elicited side-specific peripheral responses, measured as hindlimb postural asymmetry in a binary left–right output model. These neurohormonal effects were therefore transmitted via the humoral route. These findings suggest that multiple hypothalamic neurohormones and their integrated networks are asymmetrically organized, and that their lateralization may be necessary for hemisphere-specific hormonal regulation of peripheral systems.

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